Health Condition 1: G439- Migraine, unspecified
Conditions
Interventions
Intervention1: Propranolol: Oral Propranolol 40mg once daily after breakfast for duration of 4 months
Control Intervention1: Metoprolol: Oral Metoprolol 50mg once daily after breakfast for duration of
Sponsors
Dr Ramizahmad Maiyuddinbhai Mansuri
Eligibility
Inclusion criteria
Inclusion criteria: Patient will be taken as per International Headache Society Criteria for Migraine with Aura. Patient will be taken as per International Headache Society Criteria for Migraine without Aura. Patients who will be willing to take part in the study with signed and written informed consent. Patients aged between 18-65 years. Patients could be of both male and female.
Exclusion criteria
Exclusion criteria: Pregnant , breast feeding, child bearing age using contraception. Patients having asthma, bradycardia and COPD. History of Bronchospasm. Patients having Coronary Artery Diseases . Patients less than 18years & more than 65years. Patient having chronic in capacitating illness eg.AIDS,cancer,TB. Patient whose primary headaches were other than migraine headaches e.g. With a clinical history of stroke or Transient Ischemic Attack.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the efficacy of Propranolol versus Metoprolol as Prophylactic Agent in Migraine using The Migraine Disability Assessment Test and Headache Impact Test 6Timepoint: Baseline 4 weeks 8 weeks and 12 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare the Adverse drug reactions between Propranolol versus Metoprolol which will be used as prophylactic agent in Migraine by maintaining Headache DiaryTimepoint: Baseline 4 weeks 8 weeks & 12 weeks | — |
Countries
India
Contacts
Public ContactDr Devendra Singh Kushwah
Gajra Raja Medical College
Outcome results
None listed